Job Description
We’re expanding across Mexico, Brazil, Argentina, Colombia, Chile, and Peru , and we’re looking for a Principal Database Programmer to help build the foundation of our clinical data operations in LATAM. In this high‑impact role, you’ll lead the development, testing, implementation, and support of clinical databases from start-up through post‑lock, while partnering closely with Data Management, Project Management, EDC vendors, and clients.
You’ll guide database design, oversee programming activities, troubleshoot complex technical issues, support system administration, forecast project needs, and contribute to SOP and process development. This is also a unique opportunity to mentor junior programmers, train end users, support onboarding, and influence how our new regional team grows.
If you’re motivated by technical leadership, collaboration, and the chance to help shape a new regional department from the ground up, we’d love to hear from you!
Essential functions of the job include but are not limited to:
Maintains responsibility of assigned projects. Ensures on-time delivery, communicates the status of projects to internal teams and study
Maintains awareness of the key elements of the contract and scope of work for assigned project(s) and communicates status updates to the Project team as necessary.
Perform project forecasting of hours, and identification of resource requirements and manages project budgets including identification of out-of-scope work and post production changes
Provides input and guidance to the design of clinical databases to the client and internal teams
Builds and supports clinical databases
Develops, tests, and validates programs and clinical database to support client-related projects and third-party applications.
Provides system administration and advanced technical support services for internally developed applications and clinical databases, client-related projects and third-party applications
Troubleshoots and resolves software and clinical database problems
Develops and maintains study-specific validation documents
Provides support to data management for client-related projects from CRF design to post database close and archival
May design, develop and validate the Company’s internal applications, client-related projects and third-party applications.
Participate in software vendor selection
Participate in conducting EDC demonstrations and trainings
Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
Supports with onboarding of new hires
Provide leadership for cross-functional and organization-wide initiatives, where applicable
Trains and ensures that all data management project team members have been sufficiently trained
Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
Present software demonstrations/trainings, department/company training sessions, present at project meetings
Performs all duties in accordance with SOPs, government regulations, guidelines and industry standards.
May require some travel
Perform other duties as assigned
Qualifications:
Minimum Required:
Minimum 8 years’ experience
Bachelors and/or a combination of related experience
Professional working proficiency in English required
Other Required:
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
Able to handle a variety of clinical research tasks.
Excellent organizational and communication skills
Professional use of the English language; both written and oral.
Experience in Object Oriented Programming (C#, C++, VBS, etc.…),
Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.)
Experience in clinical database management system development.
Experience in a clinical, scientific or healthcare discipline.
Proficiency in more than one CDMS system to include buildi ... (truncated, view full listing at source)